2-[[5-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidenemethyl)thiophen-2-yl]methylidene]-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine | 141198-34-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩类
• 英文名称: 2-[[5-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidenemethyl)thiophen-2-yl]methylidene]-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine
• CAS: 141198-34-7
• 化学式: C₁₆H₁₂S₉
• 分子量: 492.865
• InChiKey: IQOOUXSGWVGLFG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  25
• 可旋转键数：
  2
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  231
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  2,5-噻吩二甲醛 、 (5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-yl)-phosphonic acid dimethyl ester 在 正丁基锂 作用下， 生成 2-[[5-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidenemethyl)thiophen-2-yl]methylidene]-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine
  参考文献：
  名称：

  Hansen, Thomas K.; Lakshmikantham; Cava, Nichael P., Journal of the American Chemical Society, 1992, vol. 114, # 13, p. 5035 - 5039

  摘要：

  DOI：

文献信息

• Hansen, Thomas K.; Lakshmikantham; Cava, Nichael P., Journal of the American Chemical Society, 1992, vol. 114, # 13, p. 5035 - 5039
  作者：Hansen, Thomas K.、Lakshmikantham、Cava, Nichael P.、Niziurski-Mann, Renée E.、Jensen, Frank、Becher, Jan

  DOI：——

  日期：——
• 2,5-Bis(1,4-dithiafulven-6-yl) furans, thiophenes and N-methyl pyrroles as extended analogues of tetrathiafulvalene
  作者：A.S. Benahmed-Gasmi、P. Frère、B. Garrigues、A. Gorgues、M. Jubault、R. Carlier、F. Texier

  DOI：10.1016/s0040-4039(00)79014-9

  日期：1992.10

  The title compounds are synthesized by Wittig or Wittig-Horner reactions between the corresponding furan, thiophen and N-methyl-pyrrole-2,5-dicarbaldehydes and P-reagents W or P bearing the 1,3-dithiol-2-ylidene moiety adequately substituted al the 4,5-positions; thanks to usual and thin layer cyclic voltammetry, they are shown to possess good pi-donor abilities.